Scandium triflate catalyzed ester synthesis using primary amides

Benjamin N. Atkinson; Jonathan M J Williams

doi:10.1016/j.tetlet.2014.10.124

Scandium triflate catalyzed ester synthesis using primary amides

Benjamin N. Atkinson, Jonathan M J Williams

Research output: Contribution to journal › Article › peer-review

23 Citations (SciVal)

Abstract

A scandium triflate (ScOTf)₃ catalyzed methodology has been developed to synthesize esters from primary amides. Various primary and secondary aliphatic alcohols have been shown to react in n-heptane with a range of primary amides for 24 h.

Original language	English
Pages (from-to)	6935-6938
Number of pages	4
Journal	Tetrahedron Letters
Volume	55
Issue number	50
Early online date	28 Oct 2014
DOIs	https://doi.org/10.1016/j.tetlet.2014.10.124
Publication status	Published - 10 Dec 2014

Keywords

Alcohols
Alcoholysis
Amides
Esters
Scandium

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10.1016/j.tetlet.2014.10.124

Cite this

@article{b3e5080d70d94ce1a4077faa34005fbd,

title = "Scandium triflate catalyzed ester synthesis using primary amides",

abstract = "A scandium triflate (ScOTf)3 catalyzed methodology has been developed to synthesize esters from primary amides. Various primary and secondary aliphatic alcohols have been shown to react in n-heptane with a range of primary amides for 24 h.",

keywords = "Alcohols, Alcoholysis, Amides, Esters, Scandium",

author = "Atkinson, {Benjamin N.} and Williams, {Jonathan M J}",

year = "2014",

month = dec,

day = "10",

doi = "10.1016/j.tetlet.2014.10.124",

language = "English",

volume = "55",

pages = "6935--6938",

journal = "Tetrahedron Letters",

issn = "0040-4039",

publisher = "Elsevier",

number = "50",

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TY - JOUR

T1 - Scandium triflate catalyzed ester synthesis using primary amides

AU - Atkinson, Benjamin N.

AU - Williams, Jonathan M J

PY - 2014/12/10

Y1 - 2014/12/10

N2 - A scandium triflate (ScOTf)3 catalyzed methodology has been developed to synthesize esters from primary amides. Various primary and secondary aliphatic alcohols have been shown to react in n-heptane with a range of primary amides for 24 h.

AB - A scandium triflate (ScOTf)3 catalyzed methodology has been developed to synthesize esters from primary amides. Various primary and secondary aliphatic alcohols have been shown to react in n-heptane with a range of primary amides for 24 h.

KW - Alcohols

KW - Alcoholysis

KW - Amides

KW - Esters

KW - Scandium

UR - http://www.scopus.com/inward/record.url?scp=84910618660&partnerID=8YFLogxK

UR - http://dx.doi.org/10.1016/j.tetlet.2014.10.124

U2 - 10.1016/j.tetlet.2014.10.124

DO - 10.1016/j.tetlet.2014.10.124

M3 - Article

AN - SCOPUS:84910618660

SN - 0040-4039

VL - 55

SP - 6935

EP - 6938

JO - Tetrahedron Letters

JF - Tetrahedron Letters

IS - 50

ER -

Scandium triflate catalyzed ester synthesis using primary amides

Abstract

Keywords

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Avance 300 MHz Nuclear Magnetic Resonance (NMR) Spectrometer (1South)

Avance III 400 MHz Nuclear Magnetic Resonance (NMR) Spectrometer (9West)

Electrospray Time-of-Flight Mass Spectrometer (Open-Access)

Cite this

Scandium triflate catalyzed ester synthesis using primary amides

Abstract

Keywords

Access to Document

Other files and links

Fingerprint

Equipment

Avance 300 MHz Nuclear Magnetic Resonance (NMR) Spectrometer (1South)

Avance III 400 MHz Nuclear Magnetic Resonance (NMR) Spectrometer (9West)

Electrospray Time-of-Flight Mass Spectrometer (Open-Access)

Cite this